FDA Inspection 1098055 — Fitrite Incorporated

Fitrite Incorporated — FEI 3004262563

The FDA completed an inspection of Fitrite Incorporated on Jul 31, 2019 in Quezon City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 31, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Quezon City (Philippines)

Citations

IDCFRDescription
1274721 CFR 120.8(b)(3)HACCP plan - critical limits not listed or not adequate
1814521 CFR 117.35(c)Pest control
995421 CFR 120.11(a)(1)(iv)Verification - CCP, CA record review

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.